Dielectric polyolefin compositions

ABSTRACT

Polyolefin compositions having excellent dielectric properties comprising an alkylfluoranthene having the following formula (WHEREIN R represents an alkyl group containing from 1 to 4 carbon atoms, and x is an integer of from 1 to 4, and when x is an integer of 2 or greater, R may be different or the same) in an amount of at least 0.5 parts by weight per 100 parts by weight of a polyolefin.

United States Patent [191 Takahashi et al.

DIELECTRIC POLYOLEFIN COMPOSITIONS Inventors: Masaaki Takahashi; Akira Ito;

Yuriko Igarashi, all of Tokyo; Shichiro Kawada, Ibaragi; Jiro Ogura, lbaragi; Ryoichi Ito, lbaragi, all of Japan Kureha Kagaku Kogyo Kabushiki Kaisha, Tokyo, Japan Filed: June 20, 1974 Appl. No.: 481,257

Assignee:

Foreign Application Priority Data July 3, 1973 Japan 48-74363 US. Cl 260/93.7; 117/110 PM; 252/63; 260/45.7 R; 260/873; 260/88.2 S; 260/948; 260/9496 D Int. Cl. C08F 210/00; C08F 212/00; COSF 218/00; C08F 222/00 Field of Search 260/949 GD, 93.7, 94.8, 260/882 S, 87.3, 45.7 R; 252/63, 63.2, 66

References Cited UNITED STATES PATENTS l/l963 Lemmerich et al 174/110 Primary Examiner-Joseph L. Schofer Assistant Examiner-Herbert J. Lilling Attorney, Agent, or FirmLane, Aitken, Dunner &

Ziems [57] ABSTRACT Polyolefin compositions having excellent dielectric properties comprising an alkylfluoranthene having the following formula (wherein R represents an alkyl group containing from 1 to 4 carbon atoms and x is an integer of from 1 to 4, and whenx is an integer of 2 or greater, R may be different or the same) in an amount of at least 0.5 parts by weight per 100 parts by weight of a polyolefin.

6 Claims, 4 Drawing Figures U.S. Patent Oct.28, 1975 Sheetlof4 3,915,945

FIG.

US. Patent Oct. 28, 1975 Sheet 2 of4 3,915,945

US. Patent Oct.28, 1975 Sheet4-of4 3,915,945

PHR

FIG. 4

DIELECTRIC IPOLYOLEFIN COMPOSITIONS This invention relates to a novel dielectric composition, and more particularly to a dielectric polyolefin composition which retains excellent dielectric strength over a long period of time and this is suitable for use as insulation in high voltage cables.

BACKGROUND OF THE INVENTION Polyolefins have been used in a variety of applications as insulating materials and accordingly many studies have been conducted toward improving the electrical breakdown strength of polyolefins. For exam ple US. Pat. Nos. 3,445,394 and 3,542,684 describe methods for improving electrical breakdown strength by adding various kinds of additives to the polyolefins. However, such methods have many disadvantages in that the additives used do not show good compatibility with polyolefins and that the resultant polyolefin compositions do not exhibit satisfactory properties as insulating materials, e.g., processibility, thermal stability, voltage stability, resistance to treeing which is a characteristic generally viewed as an early stage of dielectric break-down. Accordingly, a need exists to provide a novel polyolefin composition which has excellent properties as an electrical insulating material and which is free from the above-described disadvantages of the prior art.

SUMMARY OF THE INVENTION It is therefore a main object of the present invention to provide a polyolefin composition which has excellent dielectrical properties and which is particularly superior and stable in breakdown voltage strength.

The other objects and advantages, and features of the present invention will become clear from the following description.

According to the present invention, there is provided a polyolefin composition comprising as a voltage stabilizer an alkylfluoranthene having the following formula (wherein R represents an alkyl group containing from 1 to 4 carbon atoms and x is an integer of from 1 to 4, and when x is an integer of or greater, R may be different or the same) in an amount of at least 0.5 parts by weight of 100 parts by weight of a polyolefin. This polyolefin composition has excellent dielectrical properties as well as excellent processibility and resistance to weight loss which usually results from the bleeding out, sublimation or evaporation of composition components. Thus, the polyolefin composition of the present invention, when used in cables or other electrical components, offers an improved electric insulating property. The generation of voids in the molding stage is minimal. As an insulator, it resists treeing and offers improved long time voltage stability. Moreover the alkylfluoranthene does not impede the gelation of the polyolefin during the stage in which cross-linking reac tion of the polyolefin occurs.

BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a view schematically showing an instrument for determining treeing characteristic voltages of samples obtained from various kinds of polyolefin compositions of the present invention and prior art polyolefin compositions;

FIG. 2 is a graphical representation of changes in treeing characteristic voltage against lapses of time under drying conditions in hot air of C, at samples tested as in FIG. 1;

FIG. 3 is a graphical representation of the relation between the weight and drying time of the samples tested as in FIG. 1 maintained in hot air at 80C; and

FIG. 4 is a graphical representation of the relation between the amount (parts by weight) of monopropylfluoranthene per parts by weight of polyethylene, generated the treeing characteristic voltage and amount of generated bleeding.

DETAILED DESCRIPTION OF THE INVENTION The alkylfluoranthene voltage stabilizers of the present invention have the general formula wherein R represents an alkyl group containing from 1 to 4 carbon atoms and .t is an integer of from 1 to 4, provided that when x is an integer of 2 or more R may be different or the same. More particularly, the alkylfluoranthene has one to four alkyl groups selected from methyl, ethyl, propyl and butyl. These alkyl groups are bonded at arbitrary positions in the fluoranthene nucleus. The alkylfluoranthene can be easily obtained by purifying after isolation from a polycyclic aromatic hydrocarbon-rich distillate such as coal tar, petroleum tar or the like, or by reacting, for alkylation, fluoranthene with a lower olefin having four or less carbon atoms in the presence of a Friedel-crafts catalyst such as aluminium chloride or the like, or a solid acid catalyst such as silica-alumina. Though the alkylfluoranthene has generally various isomers, purity is not required; a mixture containing one or more isomers may be employed. Furthermore, the voltage stabilizer of the present invention may be a mixture of two or more alkylfluoranthenes.

The reasons for employing an alkylfluoranthene containing alkyl groups having from 1 to 4 carbon atoms are as follows: (1) fluoranthene not substituted with an alkyl group is not sufficiently compatible with a polyolefin, e.g., when a polyolefin composition using fluoranthene is prepared for use as an electrically insulating material, a bleeding occurs on the material to an excessive extent; and (2) alkylfluoranthenes, substituted with 5 or more alkyl groups (of from 1 to 4 carbon atoms), as well as those substituted with an alkyl group containing five or more carbon atoms, when mixed with a polyolefin for use as an electrically insulating material, give a lower treeing characteristic voltage and undesirable voids are generated in the material in the course of molding. Accordingly, alkylfluoranthenes other than those previously specified are not suitable for the purpose of the invention.

According to the present invention, the substituted alkylfluoranthene is used in an amount of at least 0.5,

3 preferably 0.5-l0, parts by weight per 100 parts by weight of the polyolefin. If the amount of the alkylfluoranthene per 100 parts by weight of a polyolefin is less than 0.5 parts by weight, the desired effect on voltage stability is reduced. On the other hand, if the-amount is above parts by weight, the resultant polyolefin composition may suffer from an undesirable increase of bleeding, reduction in tensile strength and loss of dielectric characteristics. Suitable polyolefins for use in the present invention include, for example, polyethylene, polypropylene, polybutene, ethylene-propylene copolymer, and ethylene-vinyl acetate copolymer. Among these, polyethylene which has been used as an insulating material for high voltage cables is preferred. The polyolefin composition of the present invention can be processed into electric-insulating materials by conventional methods. For example, when applied as an insulating material for a high voltage cable, the polyolefin composition of the present invention is mixed with a peroxide such as dicumylperoxide, l,3-bis-(tbutylperoxyisopropyl) benzene, and if necessary, an antioxidant and a filler may also be added to the composition.

EXAMPLE 1 The various voltage stabilizing additives listed in Table l were each separately mixed with 100 parts by weight of a polyethylene having a melt index of 1.2 in amounts as shown in Table 1. To each mixture was further added 2.5 parts by weight of dicumylperoxide as a cross-linking agent, and 0.2 parts by weight of 2,2,4- trimethyl-1,2-hydroquinoline polymer as an antioxidant, and the resultant mixture was kneaded by means of hotrolls at-lC for 10 min.

For comparison, similar compositions incorporating no voltage stabilizing agent and conventional voltage stabilizing additives were prepared as shown in Table 1.

Then, each of the polyethylene compositions was molded into a suitable shape. The resultant moldings were subjected to measurements of treeing characteristic voltage (KV), gelled fraction resistance to void-forming, thermal deterioration, and long time voltage stability, in accordance with the following testing methods.

(1) Determination of treeing characteristic voltage:

Each of the polyolefin compositions was pressmolded and cross-linked at a temperature of 180C for 20 min. under a pressure of 480 kg/cm to obtain a plate 1 having a size of 2.5 X 1.2 X 0.3 cm as shown in FIG. 1. Then, the cross-linking agent remaining in the plate 1 was removed by drying the plate 1 in a hot air stream at 80C for 48 hours or 1000 hours. Then, a test sample was obtained by imbedding a needle electrode 2 in our end of plate 1 to a depth so that the distance between the imbedded tip of the needle electrode 2 and the opposite end of the plate 1 was about 1 cm, as shown in FIG. 1. A number of test samples were simultaneously prepared by forming the polyolefin composition into a sheet having a thickness of 3 mm and a size of several times as large as that of the plate 1 in the same manner as described above, heat-treating the sheet to remove the cross-linking agent, imbedding a certain number of needle electrodes at a distance from each other into the sheet in the manner as mentioned above, and cutting the sheet into individual sample plates each having one needle electrode imbedded therein. The needle electrode 2 was anchored in the plate 1 by preheating-the plate 1 at 120C for 20 min.

and then imbedding the needle into the plate at C. In doing so, the resultant test sample showed no distortion. The needle electrode used in these tests had a tip end with a curvature of a radius of less than 5 p. and a tip angle of 30. Each test sample comprising a test plate 1' and needle electrode 2 was allowed to stand for 5 days and was then placed in a vessel 3, which was provided with a plate electrode 4 and filled with a No. 2 insulating oil (Japanese Industrial Standards C 2320), placing the test plate on the electrode 4. Then, a voltage was applied between the needle electrode 2 and the plate electrode 4, separated by a distance of 1 cm until a treeing formation (fracture pattern) 5 in the plate portion adjacent to the tip end of the anchored needle electrode 2 was observed. Six or eight test samples were subjected to the above single needle test while increasing the applied voltage. The voltage at which 50 of the six or eight test samples developed treeing was recorded as the treeing characteristic voltage.

(2) Gelled fraction The degree of the cross-linkage can be determined on the basis of the gelled fraction. Accordingly, by determining the gelled fraction by the following procedure, the effect of the added voltage stablizer on the degree of cross-linkage of the polyolefin can be determined.

Each of the polyolefin compositions was pressmolded and cross-linked at 180C for 20 min. under a pressure of 480 kg/cm to obtain a sheet having a thickness of about 1 mm. Then, the sheet was cut into 5 X 5 cm plates. Each plate was immersed in xylene at l 10C for about 24 hours, while replacing every 8 hours the xylene with fresh xylene, to dissolve xylene-soluble components contained in the plate. The resultant plate was further immersed overnight in methanol to extract the xylene content from the plate and then dried in a hot air stream at 80C for 48 hours. The thus dried plate was weighed and the gelled fraction was calculated as follows:

Gelled Fraction initial weight (3) Resistance to Void-forming:

The void-forming tendency of the polyolefin compositions during molding was determined.

Each of the polyolefin compositions was pressmolded using cellophane as a separating medium under controlled conditions designed to induce void-forming in the composition, i.e., at 160C for 30 min. under 20 kg/cm Then, the resultant molded sheet was cooled to 80C under the same pressure to observe the voids, if any. Test results are indicated in Table l in the following manner: a polyolefin composition producing visible voids having a size greater than 50 1.1. is indicated by a symbol x, while a composition with no voids is indicated by a symbol A.

(4) Thermal deterioration:

Each of the polyolefin compositions was pressmolded into a sheet having a thickness of about 1 mm in the same manner as in the gelled fraction testing method. The resultant sheet was cut into plates each having a size of 5 X 1.2 X 0.1 cm, which were suspended in a hot air circulating oven at C to test for resistance to thermal deterioration. A plate which showed no deterioration over a period of 20 days under 3 these conditions is designated by the symbol A, while any plate which deteriorated within 20 days is represented by a symbol (5) Long term voltage stability:

6 tect changes in treeing characteristic voltages with lapse of time. Test results are shown in FIG. 2 by way of graphs showing the relation between the drying time and treeing characteristic voltage where the plates are Where the treeing characteristic voltage, as deter- 5 dried at 80C. In FIG. 2, the abscissa shows the drying mined as under (1) above, for a sample'was 9.5 KV or time and the ordinate the treeing characteristic voltgreater after drying 80C for 1000 hours the sample is ages of the samples. In FIG. 2, curve 6 represents the represented by asymbol A, a sample having atreeing data for the test sample not containing an additive; characteristic voltage of greater than 7 KV and smaller curve 7 represents the test sample containing phenanthan 9.5 IQV by symbol B, and a sample having a threne; curve 8 represents the test sample containing treeing characteristic voltage of 6 to 7 KV by a symbol monopropylfluoranthene; and curve 9 represents the x. test sample containing pyrene. It will be apparent from Test results are shown in Table l below. It will be un' FIG. 2 that the respective treeing characteristic voltderstood from the Table that the polyethylene compoages show high values at the initial stage of drying since sitions of the present invention are superior to those unreacted cross-linking agent remains in the samples. using conventional voltage stabilizing additives. The treeing characteristic voltage is reduced with evap- Table l Additives Boiling Amount Treeing Characteristic Gelled Resistance Thermal Long term Point C (parts by voltage KV Fraction to void- Deterioravoltage weight) per Dried at Dried at 70 forming tion stability 100 parts of 80C for 80C for Polyethylene 48 hours 1000 hours Monopropyl- 400-420 1 12.3 1 1.0 92.0 A A A fluoranthene 5 16.5 13.5 87.5 A A A Dipropyl- 440-470 2 12.0 12.0 90.9 A A A fluoranthene Tripropyl- 470-510 2 11.0 11.5 91.0 A A A fluoranthene Methyl- 380-400 2 13.2 11.8 91.5 A A A fluoranthcne Ethyl- 390-410 2 13. 12.3 92.0 A A A fluoranthene Butyl- 410-450 2 9.8 10.0 91.0 A A A fluoranthcne Alkylfluoranthcnc 400-Sl0 2 12.0 1 1.5 91.3 A A A mixture I* Alkylfluoranthene 400-495 2 1 1.7 1 1.5 90.8 A A A mixture II No additive 6.3 6.2 92.0 A x x Fluoranthenc 382 1 12.0 6.5 92.3 A x x 2 13.5 6.0 92.1 A x x 5 17.0 7.2 88.3 A x x Fluorenc 295 2 10.2 6.5 68.9 X X X Pyrene 393 2 14.7 6.5 90.9 A A x Phenylnaphthalcne 358 2 12.8 7.3 83.0 A x B Sundex 81'15 w 2 7.9 6.0 83.2 x A x Notc:*Mixturc I composed of 60 W1 /0 ofmonopropylfluoranthene. M 7: ofdipropylfluoranthene. 10 wt of tripropylfluoranthene and a trace of tetrapropylfluoranthcne.

Mixture ll composed of 'i /6 of monopropylfluoranthcnc and 50 Wt 7: 0f rnonocthylfluoranthcne.

*Trade name of Sun Oil Company for a aromatic rubber solvent.

EXAMPLE 2 2 parts by weight of monopropylfiuoranthene was added to 100 parts by weight of polyethylene having a melt index of 1.2, with which were mixed 2.5 parts by weight of dicumylperoxide employed as a cross-linking agent and 0.2 parts by weight of 2,2,4-trimethyl-l,2- hydroquinoline polymer employed as an antioxidant. The resultant mixture was then kneaded by means of hot rolls at l20C for 10 min.

The above process was repeated but without the addition of voltage stabilizing additives and usin 2 parts by weight each of conventional voltage stabilizing additit es, i.e., pyrene and phenanthrene, instead of monopropylfiaoranthene. The rnonopropylfluoranthenecontaining composition, pyrene-containing composition, phenanthrene-containing composition and the composition without the additives were press-molded and cross-linl ed at a temperature of 180C for 20 min. under a pressure of 480 ltg/cm to obtain a plate having a size of 2.5 X 1.2 X 0.3 cm for each composition. The plates were placed in a hot air stream at 80C to to deoration of the cross-linking agent component after a lapse of time. It will be also apparent from the figure that since the compatibility of phenanthrene and pyrene with polyethylene is far lower than that of monopropylfluoranthene, the treeing characteristic voltage of the samples made of the phenanthrene-containing composition and the pyrene-containing composition are reduced to a degree as low as that of polyethylene composition containing no additive, within a drying time of 100 hours and of 1000 hours, respectively.

EXAMPLE 3 Test samples were prepared in the same manner as in Example 2. The test samples were placed in a hot air stream at C and changes in weight of the samples were observed over a predetermined period of time. Test results are shown in FIG. 3 by way of graphs showing the relation between the drying time and the weight of samples which are being dried at 80C. On the abscissa the drying time and on the ordinate the sample weight (grams per unit surface area.) In FIG. 3, l0 indicates the loss weight caused by evaporation of the the pyrene-containing sample; and curve 14 represents the phenanthrene-containing sample. As will be apparent from the figure, in the initial period of the drying, i.e., within the first 3 hours, the weight of the samples is rapidly reduced because of evaporation of the crosslinking agent component from each sample. The

weights of the phenanthrene-containing sample and the pyrene-containing sample were continuously reduced at a higher rate since both phenanthrene and pyrene have low affinity for polyethylene. On the other hand,

the weight of monopropylfluoranthene-containing sample was reduced relatively slowly.

EXAMPLE 4 Monopropylfluoranthene was mixed in various amounts (parts by weight) with 100 parts by weight of polyethylene. Each mixture was further mixed with 2.5 parts by weight of dicumylperoxide and 0.2 parts by weight of 2,2,4-trimethyl-1,2-hydroquino1ine polymer, and was kneaded on hot rollers at 120C for 10 min. to

obtain a polyethylene composition. Each of the compositions was molded into a plate in the same manner as in Example 2. By using the plates as a test samples, treeing characteristic voltages and amounts of bleeding were determined. Test results are shown in FIG. 4 by way of graphs showing the relation between the amount (parts by weight) of monopropylfluoranthene per 100 parts by weight of polyethylene, the treeing characteristic voltage and the amount of bleeding generated. On the abscissa is represented the amount (parts by weight) of monopropylfluoranthene per 100 parts by weight of polyethylene, while on the lefthand ordinate the treeing characteristic voltage of the samples and the righthand ordinate the amount of bleeding generated from the samples. The amount of bleeding is determined by subjecting each of the polyethylene com- 40 positions, which were used for preparing test plates, to cross-linking and press-molding to obtain a sheet having a thickness of 1 mm, drying the sheet at 80C in a hot air circulating oven for about 5 hours, placing the resultant sheet for 30 days in an atmosphere having a temperature of 25C and a relative humidity of and measuring the amount of matter bled on the surfaces of the samples. The bled amount is expressed by glcm In FIG. 4, the solid line connecting symbols 0 represents the treeing characteristic voltage, while the 50 dotted line connecting symbols A represents the bled amount. It will be apparent from FIG. 4 that though the 8 treeing characteristic voltage increase increases with additional amounts of monopropylfluoranthene, the voltage becomes almost constant after the added amount reaches 10 parts by weight. Furthermore, when the added amount is increased beyond 10 parts by weight, the amount of bleeding sharply increases.

It should be noted that the above-mentioned tendencies remain unchanged even when alkylfluoranthenes other than monopropylfluoranthene are used or when a polyolefin other than polyethylene, e.g., a ethylenebase vinyl acetate copolymer, is used together with an alkylfluoranthene. Thus, the amount of alkylfluoranthene per parts by weight of polyolefin is preferred to be within a range of 0.5 to 10 parts by weight.

EXAMPLE 5 The various alkylfluoranthenes shown in Table 2 were each separately mixed with 100 parts by weight of polyethylene having a melt index of 1.2, in the amounts shown in Table 2. Then, each of the mixtures was kneaded by means of hot rolls at C for 10 min. and was press-molded at a temperature of C for 5 min. under a pressure of 480 kg/cm to obtain a molded sample (non-cross-linked). For comparison, the above process was repeated with polyethylene alone and with polyethylene mixed with conventional additives shown in Table 2.

The thus obtained test samples were subjected to measurements of treeing characteristic voltages and long term treeing stability in the same manner as in Example l. Furthermore, the compatibility of the additives with polyethylene was determined by placing a pressed sheet having a thickness of 1 mm in a thermostatic chamber at 25C and 60 relative humidity for 30 days, wiping the bleeding from the surfaces of the sheet by means of benzene, returning the sheet to the chamber for 1 day, and measuring the weight of the test samples. Test samples which showed no or almost no weight losses are indicated by a symbol A, and test samples which showed distinctive weight losses by a symbol x.

Other tests to detect void generation, thennal deterioration and gelled fraction were not conducted since the non-cross-linked polyethylene used generally does not generate voids, and the determination of thermal deterioration and gelled fraction of the non-crosslinked polyethylene appeared meaningless.

Test results are shown in Table 2. It will be apparent from this Table that even the non-cross-linked polyethylene compositions of the present invention are far superior to those using known stabilizing additives.

Table 2 Additives Boiling Amount (parts by Treeing Characteristic Long term Compatibility Point weight) per 100 Voltage KV voltage stability "C parts of poly- Without Dried at ethylene drying 80C for 1000 hours Monopropylfluoranthcne v400420 1 12.0 12.1 A A 2 13.3 12.9 A A 5 18.5 17.6 A A Dipropylfluoranthene 440-470 2 12.5 12.0 A A Tripropylfluoranthene 470-510 2 12.3 1 1.9 A A Methylfluoranthene 380-400 2 14.0 12.5 A A Ethylfluoranthene 390-410 2 13.5 13.0 A A Butylw 12:" Table 2 -continued Additives Boiling Amount (pa rtsby I ."l'reejng Characteristic.-,. Long term I ,Compatibility Point weight) per 100 Voltage KV voltage stability "C parts of poly- 'Without' .Driedat ethylene drying 80C for-1'v 1000 hours fluoranthenc 410-450 2 10.3 9.8 A A Aklylfluoranthene Mixture 1* 400-510 2 13.3 12.2 A A Alkylfluoranthcne Mixture ll** 1 400-495 2 13.0 12.5 A A No additive 17. 3 7.0 X Fluoranthene 382 1 15.8 6.3 X X 2 21.0 7.2 x X 5 greater 7.0 X X than Fluorene 295 2 160 6.5 X X Pyrene 393 2 23.0 65 X X Phenylnaphthalene 358 2 19.5 7.0 X X Sundex 8125* 2 8.0 6.5 X A Note: Regarding, "2 *2 see Table 1.

EXAMPLE 6 A polyolefin composition of the present invention same through steam vapor at 200C, and drying the resultant cable to remove residual cross-linking agent.

The resultant cable had excellent electrical characwas formed into an insulator which comprised a wire 25 teristics as shown in Table 3.

Table 3 Cross-linked Polyethylenc* without a voltage Cross-linked Polyethylene with The expression cross-linked polyethylene without a voltage stabilizer" used refers to a cable which is made with a cross-linked polyethylene not containing dipropylfluoranthcne.

*lmpulse breakdown voltage" is the breakdown voltage value obtained by rendering the conductive layer of the cable negative and applying an initial voltage of 750 KV. In the measurement. a voltage of the same level is applied to the cable three times. and thereaficr raised by 50 RV after completion of measurement at one voltage level. As shown in the Table 3. both of the sample cables were broken down by the first application of the voltage indicated *A-C breakdown voltage was detennined by applying an initial voltage of 300 KV for 1 hour, raising the applying voltage (using a min. step rise test) in ID KV increments at 30 min. intervals until 390 KV. and (using a 1 hr. step rise test) in 10 KV increments at 1 hr. intervals after first applying a voltage of 400 KV. The time indicated in Table 3 means the period of time required to breakdown the cable was stressed to breakdown by application of voltage.

""Treeing characteristic voltage was determined by sampling a sheet having a size of 10 x 25 X 3 min" from the cable insulator and testing in the same manner as in Example 1.

cable, which comprised of a conductive material (standed wire) having a sectional area of 1000 mm The conductive wire was covered with a 2 mm thick What is claimed is: l. A dielectric composition comprising a polyolefin inner semiconductive layer, a 20 mm thick insulator and an alkylfluoranthene of the formula and a 1.5 mm thick outer semiconductive layer, in the order mentioned. The inner semiconductive layer was obtained by mixing an electrically conductive carbon black-containing ethylene-vinyl acetate copolymer with dicumylperoxide and heating the mixture to produce a cross-linked composition having a specific volume resistivity of 1 X lO Q-cm. The insulator was made from a mixture of 2 parts by weight of dipropylfluoranthene used as a voltage stabilizer and 100 parts by weight of polyethylene, which was cross-linked in the same manner as in Example 1. The outer semiconductive layer had a composition similar to the inner semiconductive layer, and a specific volume resistivity of l X IOO-cm.

The cable was prepared by simultaneously extruding the inner semiconductive layer, the insulator and the outer semiconductive layer at 120C, cross-linking the polyethylene with the extruded material by passing wherein R represents an alkyl group containing from 1 to 4 carbon atoms and x is an integer of l to 4, provided that when x is an integer of 2 or greater R may be the fluoranthene is present in an amount of 0.5 to 10 parts by weight per parts by weight of said polyolefin.

3. The composition of claim 1, wherein said alkylfluoranthene is a mixture of isomers.

4. The composition of claim 1, wherein said alkylfluoranthene is a mixture of alkylfluoranthenes.

5. The composition of claim 1, wherein said polyolefin is selected from the group consisting of polyethylene, polypropylene, polybutene, and ethylene propylene copolymers.

thene,'butylfluoranthene and mixtures thereof. 

1. A DIELECTRIC COMPOSITION COMPRISING A POLYOLEFIN AND AN ALKYLFLUORANTHENE OF THE FORMULA
 2. The composition of claim 1, wherein said alkylfluoranthene is present in an amount of 0.5 to 10 parts by weight per 100 parts by weight of said polyolefin.
 3. The composition of claim 1, wherein said alkylfluoranthene is a mixture of isomers.
 4. The composition of claim 1, wherein said alkylfluoranthene is a mixture of alkylfluoranthenes.
 5. The composition of claim 1, wherein said polyolefin is selected from the group consisting of polyethylene, polypropylene, polybutene, and ethylene propylene copolymers.
 6. The composition of claim 1, wherein said alkylfluoranthene is selected from the group consisting of methylfluoranthene, ethylfluoranthene monopropylfluoranthene, dipropylfluoranthene, tripropylfluoranthene, butylfluoranthene and mixtures thereof. 